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Article

[123I]FP-CIT SPECT findings in two patients with Hallervorden-Spatz disease with homozygous mutation in PANK2 gene.

Neurology - 11 Jan 2005

Cossu G, Cella C, Melis M, Antonini A, Floris G L, Ruffini L, Spissu A

Abstract excerpt

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Topics

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Share to PANK2 gene
Share to Homozygote
Share to Iodine Radioisotopes
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Pantothenate Kinase-Associated Neurodegeneration

Share to Phosphotransferases (Alcohol Group Acceptor)

Share to Siblings

Share to Tomography, Emission-Computed, Single-Photon

Source

Identifiers

PMID: 15642932
DOI: 10.1212/01.WNL.0000148577.62644.77

Genes

CIT
PANK2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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[123I]FP-CIT SPECT findings in two patients with Hallervorden-Spatz disease with homozygous mutation in PANK2 gene.PMID 15642932Read ↗

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A novel gene mutation in PANK2 in a patient with an atypical form of pantothenate kinase-associated neurodegeneration.Semantic proximity Read ↗

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